阿知波一雄 | Shizuoka College of Pharmacy

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著作論文

Antitumor Activity and Lethal Toxicity of Chemically Synthesized Tetraacetyl-2-keto-3-deoxyoctonic Acid-(α2→6)-D-glucosamine Analogues of Lipid A(Biological)
Comparison of Biological Activities of Chemically Synthesized Monosaccharide Analogues of Reducing and Nonreducing Sugar Moieties of Lipid A(Blological)
MITOGENIC ACTIVITY OF CHEMICALLY SYNTHESIZED TETRAACETYL-2-KETO-3-DEOXYOCTONIC ACID-(α 2→6)-D-GLUCOSAMINE ANALOGUES OF LIPID A
ANTITUMOR ACTIVITY AND BIOLOGICAL EFFECTS OF CHEMICALLY SYNTHESIZED MONOSACCHARIDE ANALOGUES OF LIPID A IN MICE
Trifluoromethanesulfonic Acid-Promoted Reaction of Hexahydro-1,3,5-triazines.Introduction of a Secondary Aminomethyl Grouping into Carboxylates at the α-Position through Ketene Silyl Acetals
Pyrrolidine-Forming 1,3-Dipolar Cycloaddition of N-(Phenylthiomethyl)-α-amino Acid Esters
1,3-DIPOLAR CYCLOADDITION LEADING TO N-ALKYLPYRROLIDINES
1,3-Dipolar Cycloaddition Leading to N-Acylated Pyrrolidines and 2,5-Dihydropyrroles
Decarboxylation Reaction. X. Introduction of a Carbon Unit at the α-Position of Amines by Reaction of Hexahydro-1,3,5-triazines with Carboxylic Acids
A 1,3-Dipolar Cycloaddition of Alicyclic Methylene Iminium Ylide to form Pyrrolizidine Nuclei and Its Application to Synthesis of Pyrrolizidine Alkaloids
TOTAL SYNTHESIS OF PROTEUS MIRABILIS LIPID A(Communication to the Editor)
Thiocarbonyl Ylides. VI, New Generation of Thiocarbonyl Ylides from Organosilicon Compounds Containing Sulfur and Their 1,3-Cycloadditions(Organic,Chemical)
Lipid A and Related Compounds. XI. New, Efficient Synthesis of Lipid X(Organic,Chemical)
EFFICIENT SYNTHESIS OF NOVEL MONOSACCHARIDE ANALOGS OF LIPIDS A
A NEW METHODOLOGY FOR CHEMOSELECTION OF ONE AMINO AND FOUR HYDROXYL GROUPS OF GLUCOSAMINE DERIVATIVES AND ITS USE FOR SYNTHESIS OF LIPID X
Enzymes and Catalysts. I. Pig Liver Esterase-Catalyzed Hydrolysis of Heterocyclic Diesters(Organic,Chemical)
Synthesis of Proline Derivatives by 1,3-Dipolar Cycloaddition of Azomethine Ylide Generated from an Organosilicon Compound(Organic,Chemical)
Evidence for Ambivalent Azomethine Ylide Intermediate in the 1, 3-Cycloaddition of Trimethylsilylmethylamine Derivatives(Organic,Chemical)
Trifluoroacetic Acid-Catalyzed 1,3-Cycloaddition of the Simplest Iminium Ylide Leading to 3-or 3,4-Substituted Pyrrolidines and 2,5-Dihydropyrroles
A DEFINITE EVIDENCE ON THE AMBIVALENT AZOMETHINE YLIDE INTERMEDIATE IN TRIFLUOROACETIC ACID- AND FLUORIDE ANION-PROMOTED 1,3-CYCLO-ADDITIONS INVOLVING THE SILICON-CARBON BOND CLEAVAGE
Highly Regioselective Synthesis of Trisubstituted Pyrrolidines by 1,3-Cydoaddition(Organic,Chemical)
One-Pot Synthesis of N-Alkylpyrrolidines by 1,3-Dipolar Cycloaddition(Organic,Chemical)
Trimethylsilyl Triflate-Catalyzed 1,3-Dipolar Cycloaddition Leading to N-Unsubstituted Pyrrolidines
1,3-Dipolar Cycloaddition of the Simplest N-Acylazomethine Ylide Leading to 3- or 3,4-Substituted N-Acylpyrrolidines
SYNTHESIS OF BIOLOGICALLY ACTIVE TETRAACETYL-3-DEOXY-D-MANNO-2-OCTULOSONIC ACID(KDO)-(α2→6)-D-GLUCOSAMINE ANALOGS OF LIPID A

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